Evidence map›Paper›PMID 40263244›Full record

ArticleInvestigational new drugs2025

The up-regulated expression level of deubiquitinating enzyme USP46 induces the apoptosis of A549 cells by TRAF6.

Xuan Zhao, Yanan Li, Dandan Gu, Xiaoru Wang, Guangxin Han, Yasen Yao, Limei Ren, Qingguo Yao, Xiaobing Li, Yonghao Qi

Abstract read
PubMed Publisher
In one paragraph

Article in Investigational new drugs, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Collagen remodeling in breast cancer progression: from molecular mechanisms to diagnostic and therapeutic opportunities.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xuan ZhaoDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Yanan LiDepartment of Neurosurgery, Second Hospital of Hebei Medical University, Shijiazhuang, 050000, Hebei, China.
Dandan GuDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Xiaoru WangDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Guangxin HanDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Yasen YaoDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Limei RenDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Qingguo YaoDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Xiaobing LiDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China.
Yonghao QiDepartment of Bioengineering, School of Chemical Engineering, Shijiazhuang University, Shijiazhuang, 050035, Hebei, China. qiyonghao1009@163.com.ORCID 0000-0003-3257-1070

Funding

Natural Science Foundation of Hebei Province No. H2022106006Shijiazhuang Science and Technology Research and Development Program No. 211200973
6 · The paper itself

Abstract

This study investigates the function of Ubiquitin-specific protease 46 (USP46), a deubiquitinase, in the context of lung cancer, particularly its role in regulating cell proliferation via the ubiquitination of TRAF6. In A549 lung cancer cells, analysis revealed a significant downregulation of USP46 expression, while TRAF6 levels were notably elevated. These findings were corroborated by Western blotting, which confirmed the altered expression patterns. To further assess the implications of these changes, several experimental assays, including the Cell Counting Kit-8, transwell migration assays, and flow cytometry, were conducted to evaluate cell viability and apoptosis rates. Co-immunoprecipitation experiments demonstrated a direct interaction between USP46 and TRAF6, implicating USP46 in the modulation of TRAF6 ubiquitination, a process that is fundamental to tumor physiology. The results indicated that decreased USP46 expression led to an increase in the levels of the anti-apoptotic protein Bcl-2, while there was a corresponding decrease in key pro-apoptotic proteins such as caspase-3, caspase-9, and Bax. Additionally, the study found elevated levels of phosphorylated AKT and mTOR, which suggest the activation of survival signaling pathways in the cancer cells. These findings collectively suggest that the up-regulated USP46 promotes apoptosis in lung cancer cells through the regulation of TRAF6. Therefore, targeting the USP46/TRAF6 signaling pathway presents a promising therapeutic strategy for lung cancer treatment, potentially offering new avenues for intervention in cancer progression and cell survival mechanisms.

Indexed as

ApoptosisEndopeptidasesLung NeoplasmsTNF Receptor-Associated Factor 6A549 CellsCell ProliferationCell SurvivalHumansIntracellular Signaling Peptides and ProteinsProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesUbiquitinationUp-RegulationEndopeptidasesIntracellular Signaling Peptides and ProteinsProto-Oncogene Proteins c-aktTifab protein, humanTNF Receptor-Associated Factor 6TOR Serine-Threonine KinasesA549ApoptosisDeubiquitinating enzymeTRAF6USP46

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.